CNS pathology course Recommended textbook: Vinay Kumar, Abul K. Abbas, Nelson Fausto, & Richard Mitchell , Robbins Basic Pathology, 8th Edition The course guidelines including the lectures contents are very important. Make sure to read them carefully. You are requested to study all the Key principles, even if they were not discussed in the lectures.

CNS Tumors Pathology

CNS Tumors Incidence The annual incidence of tumors of the CNS ranges from: 10 to 17 per 100,000 persons for intracranial tumors 1 to 2 per 100,000 persons for intraspinal tumors About half to three-quarters are primary tumors, and the rest are metastatic

CNS Tumors and childhood Tumors of the CNS are a larger proportion of cancers of childhood, accounting for as many of 20% of all tumors CNS tumors in childhood differ from those in adults both in histologic subtype and location In childhood, tumors are likely to arise in the posterior fossa, while in adults they are mostly supratentorial

CNS Tumors General characteristics The anatomic site of the neoplasm can have lethal consequences irrespective of histological classification (i.e. benign tumors can be fatal in certain locations)  examples on such locations? The pattern of spread of primary CNS neoplasms differs from that of other tumors: rarely metastasize outside the CNS the subarachnoid space does provide a pathway for spread  What are the layers that surround subarachnoid space?

CNS Tumors General manifestations Seizures, headaches, vague symptoms Focal neurologic deficits related to the anatomic site of involvement Rate of growth may correlate with history

CNS tumors Classification May arise from: cells of the coverings (meningiomas) cells intrinsic to the brain (gliomas, neuronal tumors, choroid plexus tumors) other cell populations within the skull (primary CNS lymphoma, germ-cell tumors) they may spread from elsewhere in the body (metastases)

CNS Tumors Gliomas Astrocytomas Oligodendrogliomas Ependymomas

CNS Tumors Astrocytomas Fibrillary: 4th to 6th decade Commonly cerebral hemisphere Variable grades: Diffuse astrocytoma Anaplstic astrocytoma Glioblastoma Pilocytic Children and young adults Commonly cerebellum Relatively benign

CNS Tumors Fibrillary Astrocytoma Well differentiated “diffuse astrocytoma” (WHO grade II) : Static or progress slowly (mean survival of more than 5 years) Moderate cellularity Variable nuclear pleomorphism Less differentiated (higher-grade) : Anaplstiac astrocytoma (WHO grade III) More cellular Greater nuclear pelomrophism Mitosis Glioblastoma (WHO grade IV) With treatment, mean survival of 8-10 months Necrosis and/or vascular or endothelial cell proliferation

Note that diffuse astrocytoma are poorly demarcated

GBM Pseudopalisading necrosis AND/OR Vascular proliferation Edema and vascular leak WHO grading

CNS Tumors Glioblastoma It became clear that secondary glioblastomas shared p53 mutations that characterized low-grade gliomas While primary glioblastomas were characterized by amplification of the epidermal growth factor receptor (EGFR) gene

CNS Tumors Pilocytic Astrocytoma Often cystic, with a mural nodule Well circumscribed "hairlike“=pilocytic processes that are GFAP positive Rosenthal fibers & hyaline granular bodies are often present Necrosis and mitoses are typically absent

CNS Tumors Oligodendroglioma The most common genetic findings are loss of heterozygosity for chromosomes 1p and 19q Fourth and fifth decades Cerebral hemispheres, with a predilection for white matter Better prognosis than do patients with astrocytomas (5 to 10 years with Rx) Anaplastic form prognosis is worse

In oligodendroglioma tumor cells have round nuclei, often with a cytoplasmic halo Blood vessels in the background are thin and can form an interlacing pattern What additional features are needed for anaplastic oligodendroglioma?

CNS Tumors Ependymoma Most often arise next to the ependyma-lined ventricular system, including the central canal of the spinal cord The first two decades of life, they typically occur near the fourth ventricle In adults, the spinal cord is their most common location

CNS Tumors Ependymoma Tumor cells may form round or elongated structures (rosettes, canals)  what is a rosette? perivascular pseudo-rosettes Anaplastic ependymomas show increased cell density, high mitotic rates, necrosis and less evident ependymal differentiation

CNS Tumors Meningioma Predominantly benign tumors of adults Origin: meningothelial cell of the arachnoid

CNS Tumors Meningioma Well demarcated Attached to the dura with compression of underlying brain Whorled pattern of cell growth and psammoma bodies

CNS Tumors Meningioma Main subtypes: Also note: Syncytial Fibroblastic Transitional Also note: Atypical meningiomas Anaplastic (malignant) meningiomas

CNS Tumors Meningioma Although most meningiomas are easily separable from underlying brain, some tumors infiltrate the brain. The presence of brain invasion is associated with increased risk of recurrence.

CNS Tumors Medulloblastoma Children and exclusively in the cerebellum Neuronal and glial markers may be expressed, but the tumor is often largely undifferentiated The tumor is highly malignant, and the prognosis for untreated patients is dismal; however, it is exquisitely radiosensitive With total excision and radiation, the 5-year survival rate may be as high as 75%

CNS Tumors Medulloblastoma extremely cellular, with sheets of anaplastic ("small blue") cells small, with little cytoplasm and hyperchromatic nuclei; mitoses are abundant.

Nervous system Tumors Schwannoma Benign In the CNS, they are often encountered within the cranial vault in the cerebellopontine angle, where they are attached to the vestibular branch of the eighth nerve (tinnitus and hearing loss) Bilateral = NF2

Nervous system Tumors Schwannoma Sporadic schwannomas are associated with mutations in the NF2 gene Bilateral acoustic schwannoma is associated with NF2 Attached to the nerve but can be separated from it

Nervous system Tumors Schwannoma Cellular Antoni A pattern and less cellular Antoni B nuclear-free zones of processes that lie between the regions of nuclear palisading are termed Verocay bodies

Nervous system Tumors Neurofibroma Examples: (cutaneous neurofibroma) or in peripheral nerve (solitary neurofibroma) These arise sporadically or in association with type 1 neurofibromatosis, rarely malignant plexiform neurofibroma, mostly arising in individuals with NF1, potential malignancy Neurofibromas cannot be separated from nerve trunk (in comparison to shcwannoma)

Nervous system Tumors Metastatic tumours About half to three-quarters of brain tumors are primary tumors, and the rest are metastatic Lung, breast, skin (melanoma), kidney, and gastrointestinal tract are the commonest

Homework! FAMILIAL TUMOR SYNDROMES - Describe the inheritance pattern and the main features of: Type 1 Neurofibromatosis Type 2 Neurofibromatosis Which one of these two syndromes, has a propensity for the neurofibromas to undergo malignant transformation at a higher rate than that observed for comparable tumors in the general population? Tip: use the recommended textbook and the internet.